Formations of, Acquisitions by, and Mergers of Bank Holding Companies, 50037-50038 [2019-20564]
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Federal Register / Vol. 84, No. 185 / Tuesday, September 24, 2019 / Notices
application Form FMC–18, and the
related foreign-based unlicensed
NVOCC registration/renewal Form
FMC–65.
Type of Request: Reinstatement, with
changes of a previously approved
collection for which approval has
expired.
Proposed Changes: The proposed
changes to the collection reflect
proposed changes to Part 515 in a recent
rulemaking, which include: (a)
Removing optional paper license
application process and related
reference to fee amounts; (b) clarifying
language specifying who can be the
Qualifying Individual in a partnership
between entities other than individuals;
(c) updating description of processes
regarding renewals, bonds, and
terminations; (d) expanding the types of
applications subject to direct
Commission review to include
applicants employing the same officers,
managers, or members of an OTI whose
license was revoked or denied within
the previous three years; (e) clarifying
that sureties provide the organization
number of OTIs with claim details for
registered NVOCCs; (f) adding the
submission of Form FMC–1 prior to
being licensed; and (g) deleting
reference to availability of the Regulated
Person’s Index (RPI) upon request.
Most of the proposed changes seek to
streamline licensing, registration,
renewal, and termination processes so
that the Commission, licensees and
registrants can receive and transmit
documents electronically; remove
references to paper license application
and registration forms on the basis that
no requests for waivers of electronic
filing requirement were received; and
assist carriers in verifying an NVOCC’s
compliance with OTI licensing, tariff,
and financial responsibility
requirements by adding the requirement
that Form FMC–1 be submitted prior to
issuance of an OTI license. Electronic
filing of applications, registrations, and
financial responsibility documents
reduces cost to OTIs and the
Commission and facilitates Commission
review and issuance of OTI licenses and
registrations. The Commission currently
issues OTI licenses upon receipt of
evidence of financial responsibility.
Licensees that are NVOCCs must
publish a tariff and notify the
Commission using Form FMC–1, prior
to commencing NVOCC service. The
proposed change to issue an NVOCC
OTI license upon receipt of financial
responsibility and Form FMC–1 will
assist common carriers in determining
an NVOCC’s compliance with the OTI
licensing, tariff, and financial
responsibility requirements. Foreign-
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registered NVOCCs submit a Form
FMC–65, Form FMC–1, and evidence of
financial responsibility to the
Commission prior to commencing
NVOCC service. The Commission is
clarifying that sureties provide the
organization number of OTIs with claim
details for registered NVOCCs. The
sureties currently provide similar
identifying information for licensed
OTIs. Data contained in the RPI can be
downloaded at no cost from the
Commission’s website, and therefore the
Commission is proposing to delete
reference to availability of the RPI upon
request.
Purpose: The Commission uses
information obtained under this part
and through Form FMC–18 to determine
the qualifications of OTIs and their
compliance with the Act and
regulations, and to enable the
Commission to discharge its duties
under the Act by ensuring that OTIs
maintain acceptable evidence of
financial responsibility. If the collection
of information were not conducted,
there would be no basis upon which the
Commission could determine if
applicants are qualified for licensing.
The Commission would also not be able
to effectively assess the compliance of
foreign-based, unlicensed NVOCCs
without the required registration
information.
Frequency: This information is
collected when applicants apply for a
license or submit a registration,
complete the triennial renewal, or when
existing licensees or registrants change
certain information in their application
forms.
Type of Respondents: The types of
respondents are persons desiring to
obtain or maintain a license or
registration to act as an OTI. Under the
Act, OTIs may be either an ocean freight
forwarder, a non-vessel-operating
common carrier, or both.
Number of Annual Respondents: The
Commission estimates a potential
annual respondent universe of 6,475
entities.
Estimated Time per Response: The
time per response to complete
application Form FMC–18 averages 2
hours and to complete the triennial
renewal is 10 minutes. The time to
complete a financial responsibility form
averages 20 minutes. The time to
complete Form FMC–65 to submit or
renew a registration as a foreign-based,
unlicensed NVOCC averages 10
minutes.
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50037
Total Annual Burden: The
Commission estimates the total annual
burden at 3,918 hours.
Rachel Dickon,
Secretary.
[FR Doc. 2019–20614 Filed 9–23–19; 8:45 am]
BILLING CODE 6731–AA–P
FEDERAL RESERVE SYSTEM
Formations of, Acquisitions by, and
Mergers of Bank Holding Companies
The companies listed in this notice
have applied to the Board for approval,
pursuant to the Bank Holding Company
Act of 1956 (12 U.S.C. 1841 et seq.)
(BHC Act), Regulation Y (12 CFR part
225), and all other applicable statutes
and regulations to become a bank
holding company and/or to acquire the
assets or the ownership of, control of, or
the power to vote shares of a bank or
bank holding company and all of the
banks and nonbanking companies
owned by the bank holding company,
including the companies listed below.
The applications listed below, as well
as other related filings required by the
Board, are available for immediate
inspection at the Federal Reserve Bank
indicated. The applications will also be
available for inspection at the offices of
the Board of Governors. Interested
persons may express their views in
writing on the standards enumerated in
the BHC Act (12 U.S.C. 1842(c)). If the
proposal also involves the acquisition of
a nonbanking company, the review also
includes whether the acquisition of the
nonbanking company complies with the
standards in section 4 of the BHC Act
(12 U.S.C. 1843), and interested persons
may express their views in writing on
the standards enumerated in section 4.
Unless otherwise noted, nonbanking
activities will be conducted throughout
the United States.
Comments regarding each of these
applications must be received at the
Reserve Bank indicated or the offices of
the Board of Governors, Ann E.
Misback, Secretary of the Board, 20th
and Constitution Avenue NW,
Washington, DC 20551–0001, not later
than October 24, 2019.
A. Federal Reserve Bank of Chicago
(Colette A. Fried, Assistant Vice
President) 230 South LaSalle Street,
Chicago, Illinois 60690–1414:
1. Central Bancshares, Inc.,
Muscatine, Iowa; to acquire the
outstanding voting shares of Walcott
Trust & Savings Bank, Walcott, Iowa,
pursuant to section 3 of the Bank
Holding Company Act. In connection
with this application, Central
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50038
Federal Register / Vol. 84, No. 185 / Tuesday, September 24, 2019 / Notices
Bancshares, Inc., has applied to acquire
Hail, Inc., Walcott, Iowa, and thereby
engage in the sale of insurance in a town
of less than 5,000 in population
pursuant to section 4 of the Bank
Holding Company Act and 12 CFR
225.28(b)(11)(iii)(A).
Board of Governors of the Federal Reserve
System, September 18, 2019.
Yao-Chin Chao,
Assistant Secretary of the Board.
[FR Doc. 2019–20564 Filed 9–23–19; 8:45 am]
BILLING CODE 6210–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2019–N–1215]
Post-Marketing Pediatric-Focused
Product Safety Reviews;
Establishment of a Public Docket;
Request for Comments
AGENCY:
Food and Drug Administration,
HHS.
Notice, establishment of a
public docket; request for comments.
ACTION:
The Food and Drug
Administration (FDA) is establishing a
public docket to collect comments
related to the post-marketing pediatricfocused safety reviews of products
posted between April 12, 2019, and
September 23, 2019, on FDA’s website
but not presented at the September 26
or 27, 2019, Joint Pediatric Advisory
Committee (PAC) and Drug Safety and
Risk Management (DSaRM) Advisory
Committee meeting. These reviews are
intended to be available for review and
comment by members of the PAC,
interested parties (such as academic
researchers, regulated industries,
consortia, and patient groups), and the
general public.
DATES: Submit either electronic or
written comments by October 7, 2019.
ADDRESSES: FDA is establishing a docket
for public comment on this document.
The docket number is FDA–2019–N–
1215. The docket will close on October
7, 2019. Submit either electronic or
written comments by that date. Please
note that late, untimely comments will
not be considered. Electronic comments
must be submitted on or before October
7, 2019. The https://
www.regulations.gov electronic filing
system will accept comments until
midnight Eastern Time at the end of
October 7, 2019. Comments received by
mail/hand delivery/courier (for written/
paper submissions) will be considered
timely if they are postmarked or the
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SUMMARY:
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delivery service acceptance receipt is on
or before that date.
You may submit comments as
follows:
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
Comments submitted electronically,
including attachments, to https://
www.regulations.gov will be posted to
the docket unchanged. Because your
comment will be made public, you are
solely responsible for ensuring that your
comment does not include any
confidential information that you or a
third party may not wish to be posted,
such as medical information, your or
anyone else’s Social Security number, or
confidential business information, such
as a manufacturing process. Please note
that if you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be
posted on https://www.regulations.gov.
• If you want to submit a comment
with confidential information that you
do not wish to make available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand Delivery/Courier (for
written/paper submissions): Dockets
Management Staff (HFA–305), Food and
Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Dockets Management
Staff, FDA will post your comment, as
well as any attachments, except for
information submitted, marked and
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2019–N–1215 for ‘‘Post-Marketing
Pediatric-Focused Product Safety
Reviews; Establishment of a Public
Docket; Request for Comments.’’
Received comments, those filed in a
timely manner (see ADDRESSES), will be
placed in the docket and, except for
those submitted as ‘‘Confidential
Submissions,’’ publicly viewable at
https://www.regulations.gov or at the
Dockets Management Staff between 9
a.m. and 4 p.m., Monday through
Friday.
• Confidential Submissions—To
submit a comment with confidential
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information that you do not wish to be
made publicly available, submit your
comments only as a written/paper
submission. You should submit two
copies total. One copy will include the
information you claim to be confidential
with a heading or cover note that states
‘‘THIS DOCUMENT CONTAINS
CONFIDENTIAL INFORMATION.’’ FDA
will review this copy, including the
claimed confidential information, in its
consideration of comments. The second
copy, which will have the claimed
confidential information redacted/
blacked out, will be available for public
viewing and posted on https://
www.regulations.gov. Submit both
copies to the Dockets Management Staff.
If you do not wish your name and
contact information to be made publicly
available, you can provide this
information on the cover sheet and not
in the body of your comments and you
must identify this information as
‘‘confidential.’’ Any information marked
as ‘‘confidential’’ will not be disclosed
except in accordance with 21 CFR 10.20
and other applicable disclosure law. For
more information about FDA’s posting
of comments to public dockets, see 80
FR 56469, September 18, 2015, or access
the information at: https://www.gpo.gov/
fdsys/pkg/FR-2015-09-18/pdf/201523389.pdf.
Docket: For access to the docket to
read background documents or the
electronic and written/paper comments
received, go to https://
www.regulations.gov and insert the
docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
and/or go to the Dockets Management
Staff, 5630 Fishers Lane, Rm. 1061,
Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT:
Marieann Brill, Office of the
Commissioner, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 32, Rm. 5154, Silver Spring,
MD 20993, 240–402–3838,
marieann.brill@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: FDA is
responsible for protecting the public
health by assuring the safety, efficacy,
and security of human and veterinary
drugs, biological products, medical
devices, our Nation’s food supply,
cosmetics, and products that emit
radiation. FDA also has responsibility
for regulating the manufacturing,
marketing, and distribution of tobacco
products to protect the public health
and to reduce tobacco use by minors.
FDA is establishing a public docket,
Docket No. FDA–2019–N–1215, to
receive input on post-marketing
pediatric-focused safety reviews of
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Agencies
[Federal Register Volume 84, Number 185 (Tuesday, September 24, 2019)]
[Notices]
[Pages 50037-50038]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-20564]
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FEDERAL RESERVE SYSTEM
Formations of, Acquisitions by, and Mergers of Bank Holding
Companies
The companies listed in this notice have applied to the Board for
approval, pursuant to the Bank Holding Company Act of 1956 (12 U.S.C.
1841 et seq.) (BHC Act), Regulation Y (12 CFR part 225), and all other
applicable statutes and regulations to become a bank holding company
and/or to acquire the assets or the ownership of, control of, or the
power to vote shares of a bank or bank holding company and all of the
banks and nonbanking companies owned by the bank holding company,
including the companies listed below.
The applications listed below, as well as other related filings
required by the Board, are available for immediate inspection at the
Federal Reserve Bank indicated. The applications will also be available
for inspection at the offices of the Board of Governors. Interested
persons may express their views in writing on the standards enumerated
in the BHC Act (12 U.S.C. 1842(c)). If the proposal also involves the
acquisition of a nonbanking company, the review also includes whether
the acquisition of the nonbanking company complies with the standards
in section 4 of the BHC Act (12 U.S.C. 1843), and interested persons
may express their views in writing on the standards enumerated in
section 4. Unless otherwise noted, nonbanking activities will be
conducted throughout the United States.
Comments regarding each of these applications must be received at
the Reserve Bank indicated or the offices of the Board of Governors,
Ann E. Misback, Secretary of the Board, 20th and Constitution Avenue
NW, Washington, DC 20551-0001, not later than October 24, 2019.
A. Federal Reserve Bank of Chicago (Colette A. Fried, Assistant
Vice President) 230 South LaSalle Street, Chicago, Illinois 60690-1414:
1. Central Bancshares, Inc., Muscatine, Iowa; to acquire the
outstanding voting shares of Walcott Trust & Savings Bank, Walcott,
Iowa, pursuant to section 3 of the Bank Holding Company Act. In
connection with this application, Central
[[Page 50038]]
Bancshares, Inc., has applied to acquire Hail, Inc., Walcott, Iowa, and
thereby engage in the sale of insurance in a town of less than 5,000 in
population pursuant to section 4 of the Bank Holding Company Act and 12
CFR 225.28(b)(11)(iii)(A).
Board of Governors of the Federal Reserve System, September 18,
2019.
Yao-Chin Chao,
Assistant Secretary of the Board.
[FR Doc. 2019-20564 Filed 9-23-19; 8:45 am]
BILLING CODE 6210-01-P